Human Albumin 20% 100 ml

Indonesia • Ferron Par Pharmaceuticals


Increase in oncotic pressure in case of oncotic deficiency. Diluted as a 4-5% solution for iso-oncotic volume replacement with long-term effect. Therapy of albumin deficiency.


Human Albumin 20.000 mg


1 bottle of 100 ml

Dosage Forms

IV Infusion

ATC Classification



Consult Your Doctor
Safety of this item for use with alcohol has not been established. Please consult your doctor.
Safe if Prescribed
This item is safe for use while operating heavy machinery.
Safe if Prescribed
This item is safe for use during pregnancy.
Safe if Prescribed
This item is safe for use during lactation.


For All Ages

Human albumin can be administered by the intravenous route, either undiluted or after dilution in an isotonic solution (e.g. 5% glucose or 0.9 % sodium chloride).

Albumin solutions must not be diluted with water for injections as this may cause haemolysis in recipients. The infusion rate should be adjusted according to the individual circumstances and the indication.

In plasma exchange the infusion-rate should be adjusted to the rate of removal. If large volumes are administered, the product should be warmed to room or body temperature before use. Do not use solutions which are cloudy or contain residues (deposits/particles). This may indicate that the protein is unstable or that the solution has become contaminated

Other Details

The dose required depends on the size of the patient, the severity of trauma or illness and on continuing fluid and protein losses. Measures of adequacy of circulating volume and not plasma albumin levels should be used to determine the dose required.

If human albumin is to be administered, hemodynamic performance should be monitored regularly; this may include:

  • arterial blood pressure and pulse rate
  • central venous pressure
  • pulmonary artery wedge pressure
  • urine output
  • electrolyte
  • haematocrit/haemoglobin